01 1AUROBINDO PHARMA LIMITED Hyderabad IN
02 1MYLAN LABORATORIES LIMITED Hyderabad IN
01 2Didanosine
01 1India
02 1U.S.A
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2007-301 - Rev 02
Status : Valid
Issue Date : 2017-02-03
Type : Chemical
Substance Number : 2200
Certificate Number : R0-CEP 2013-356 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2017-09-18
Type : Chemical
Substance Number : 2200
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PharmaCompass offers a list of Didanosine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Didanosine manufacturer or Didanosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Didanosine manufacturer or Didanosine supplier.
PharmaCompass also assists you with knowing the Didanosine API Price utilized in the formulation of products. Didanosine API Price is not always fixed or binding as the Didanosine Price is obtained through a variety of data sources. The Didanosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Videx EC;Videx manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Videx EC;Videx, including repackagers and relabelers. The FDA regulates Videx EC;Videx manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Videx EC;Videx API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Videx EC;Videx supplier is an individual or a company that provides Videx EC;Videx active pharmaceutical ingredient (API) or Videx EC;Videx finished formulations upon request. The Videx EC;Videx suppliers may include Videx EC;Videx API manufacturers, exporters, distributors and traders.
click here to find a list of Videx EC;Videx suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Videx EC;Videx CEP of the European Pharmacopoeia monograph is often referred to as a Videx EC;Videx Certificate of Suitability (COS). The purpose of a Videx EC;Videx CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Videx EC;Videx EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Videx EC;Videx to their clients by showing that a Videx EC;Videx CEP has been issued for it. The manufacturer submits a Videx EC;Videx CEP (COS) as part of the market authorization procedure, and it takes on the role of a Videx EC;Videx CEP holder for the record. Additionally, the data presented in the Videx EC;Videx CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Videx EC;Videx DMF.
A Videx EC;Videx CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Videx EC;Videx CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Videx EC;Videx suppliers with CEP (COS) on PharmaCompass.
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